Canonical Allele Identifier: CA2264360626
Gene: NME1 HGNC NCBI
NME1-NME2 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.51153553A= , CM000679.2:g.51153553A= GRCh38
NC_000017.10:g.49230914A= , CM000679.1:g.49230914A= GRCh37
NC_000017.9:g.46585913A= NCBI36
NG_021169.1:g.4995A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000393196.7:c.-114A= (NME1) ENSP00000376892.3:n.-114A=
NM_001018136.2:c.-114A= (NME1-NME2) NP_001018146.1:n.-114A=
NR_037149.1:n.18A= (NME1-NME2)
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